NR1D2 - nuclear receptor subfamily 1 group D member 2 Gene

Also Known as RVR; BD73; EAR-1R; REVERBB; REVERBbeta

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 9975

About NR1D2

Cytogenetic location: 3p24.2 Genomic coordinates (GRCh38): 3:23,945,286-23,980,617 (from NCBI)

This gene has 5 transcripts (splice variants), 474 orthologues and 18 paralogues. Ubiquitous expression in thyroid (RPKM 35.4), ovary (RPKM 18.9) and 25 other tissues.

Summary

This gene encodes a member of the nuclear hormone receptor family, specifically the NR1 subfamily of receptors. The encoded protein functions as a transcriptional repressor and may play a role in circadian rhythms and carbohydrate and lipid metabolism. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]

NR1D2 Products (2)

mRNA Protein Name
NM_001145425.2 NP_001138897.1 nuclear receptor subfamily 1 group D member 2 isoform 2
NM_005126.5 NP_005117.3 nuclear receptor subfamily 1 group D member 2 isoform 1
Molecular Function GO Annotation Evidence References Source
enables RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA
IDA: Inferred from direct assay
17892483 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17892483 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 GOA
Biological Process GO Annotation Evidence References Source
involved in negative regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
17892483 GOA
Cellular Component GO Annotation Evidence References Source
located in nucleus IDA
IDA: Inferred from direct assay
17892483 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

NR1D2 Protein Structure

zf-C4

zf-C4: Zinc finger, C4 type (two domains) (102 - 171)

Hormone_recep

Hormone_recep: Ligand-binding domain of nuclear hormone receptor (394 - 575)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 579 a.a.
Protein Preferred Names Protein Names

nuclear receptor subfamily 1 group D member 2

  • V-erbA-related protein 1-related

NR1D2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
NR1D2 Q14995 KIF1B Homo sapiens O60333-2 32814053
Intra
NR1D2 Q14995 KIF1B Homo sapiens O60333-2 32814053
Intra
NR1D2 Q14995 KIF1B Homo sapiens O60333-2 32814053
Intra
NR1D2 Q14995 DMWD Homo sapiens G5E9A7 32814053
Intra
NR1D2 Q14995 DMWD Homo sapiens G5E9A7 32814053
Intra
NR1D2 Q14995 DMWD Homo sapiens G5E9A7 32814053
Intra
NR1D2 Q14995 GRN Homo sapiens P28799-2 32814053
Intra
NR1D2 Q14995 GRN Homo sapiens P28799-2 32814053
Intra
NR1D2 Q14995 GRN Homo sapiens P28799-2 32814053
Intra
NR1D2 Q14995 q9y649_human Homo sapiens Q9Y649 32814053
Intra
NR1D2 Q14995 q9y649_human Homo sapiens Q9Y649 32814053
Intra
NR1D2 Q14995 q9y649_human Homo sapiens Q9Y649 32814053
Intra
NR1D2 Q14995 FGFR3 Homo sapiens P22607 32814053
Intra
NR1D2 Q14995 FGFR3 Homo sapiens P22607 32814053
Intra
NR1D2 Q14995 FGFR3 Homo sapiens P22607 32814053
Intra
NR1D2 Q14995 GSN Homo sapiens P06396 32814053
Intra
NR1D2 Q14995 GSN Homo sapiens P06396 32814053
Intra
NR1D2 Q14995 GSN Homo sapiens P06396 32814053
Intra
NR1D2 Q14995 HSPB1 Homo sapiens P04792 32814053
Intra
NR1D2 Q14995 HSPB1 Homo sapiens P04792 32814053
Intra
NR1D2 Q14995 HSPB1 Homo sapiens P04792 32814053
Intra
NR1D2 Q14995 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
NR1D2 Q14995 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
NR1D2 Q14995 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
NR1D2 Q14995 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
NR1D2 Q14995 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
NR1D2 Q14995 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
NR1D2 Q14995 SPRED1 Homo sapiens Q7Z699 32814053
Intra
NR1D2 Q14995 SPRED1 Homo sapiens Q7Z699 32814053
Intra
NR1D2 Q14995 SPRED1 Homo sapiens Q7Z699 32814053
Intra
NR1D2 Q14995 WFS1 Homo sapiens O76024 32814053
Intra
NR1D2 Q14995 WFS1 Homo sapiens O76024 32814053
Intra
NR1D2 Q14995 WFS1 Homo sapiens O76024 32814053
Intra
NR1D2 Q14995 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
NR1D2 Q14995 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
NR1D2 Q14995 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
NR1D2 Q14995 GRN Homo sapiens P28799 32814053
Intra
NR1D2 Q14995 GRN Homo sapiens P28799 32814053
Intra
NR1D2 Q14995 GRN Homo sapiens P28799 32814053
Cross
NR1D2 Q14995 Clock Mus musculus O08785 23555304
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Atrioventricular Septal Defect
  • AVSD

  • Atrioventricular Canal Defect

  • Avcd

  • Endocardial Cushion Defect

  • Ecd

  • Avc Defect

  • Atrioventricular Septal Defect, Susceptibility To, 1

  • Atrioventricular Septal Defect 1

  • Endocardial Cushion Defects

  • Septal Defect, Atrioventricular

  • Atrioventricular Defect With Atrial Shunting Only

  • Incomplete Atrioventricular Septal Defect With Isolated Atrial Component

  • Incomplete Atrioventricular Canal Defect With Isolated Atrial Component

  • Primum Atrial Septal Defect

  • Partial Atrioventricular Canal Defect With Isolated Atrial Component

  • Partial Atrioventricular Septal Defect, Ostium Primum Type

  • Ostium Primum Atrial Septal Defect

  • Partial Atrioventricular Canal Defect

  • Partial Atrioventricular Septal Defect

  • Atrial Septum Primum Defect

  • Atrioventricular Canal Defect With Isolated Ventricular Component

  • Atrioventricular Canal Defect With Isolated Ventricular Communication

  • Atrioventricular Septal Defect With Isolated Ventricular Component

  • Atrioventricular Septal Defect With Atrial Shunting And Restrictive Ventricular Shunting

  • Intermediate Atrioventricular Canal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valve

  • Transitional Atrioventricular Septal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valves

  • Atrioventricular Canal Defect Associated With A Restrictive Ventricular Septal Defect

  • Intermediate Atrioventricular Canal Defect

  • Intermediate Atrioventricular Septal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valvar Orifices

  • Intermediate Atrioventricular Septal Defect

  • Transitional Atrioventricular Canal Defect

  • Transitional Atrioventricular Septal Defect

  • Complete Atrioventricular Canal With Atrial And Ventricular Components

  • Complete Atrioventricular Canal Defect

  • Complete Atrioventricular Septal Defect

Delayed Sleep Phase Disorder
  • Delayed Sleep Phase Syndrome

  • Delayed Sleep Phase Syndrome, Susceptibility To

  • DSPD

  • Delayed Sleep Phase Disorder, Susceptibility To

  • DSPS

  • Sleep Phase, Delayed, Disorder

  • Sleep Phase Syndrome, Delayed, Susceptibility To

Advanced Sleep Phase Syndrome
  • Fasps

  • Familial Advanced Sleep-Phase Syndrome

  • Advanced Sleep Phase Syndrome, Familial

  • Familial Advanced Sleep Phase Syndrome

  • Sleep Phase Syndrome, Advanced, Familial

  • Advanced Sleep-Phase Syndrome, Familial

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus NR1D2 MGD MGI:2449205
Canis familiaris NR1D2 VGNC VGNC:43941
Felis catus NR1D2 VGNC VGNC:68543
Macaca mulatta NR1D2 VGNC VGNC:75503
Bos taurus NR1D2 VGNC VGNC:32229
Rattus norvegicus NR1D2 RGD RGD:628828
Others NR1D2 NCBI